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阿维鲁单抗+阿昔替尼与舒尼替尼作为晚期肾细胞癌患者一线治疗的比较:III期JAVELIN Renal 101试验的最终分析

Avelumab + axitinib versus sunitinib as first-line treatment for patients with advanced renal cell carcinoma: final analysis of the phase III JAVELIN Renal 101 trial.

作者信息

Choueiri T K, Penkov K, Uemura H, Campbell M T, Pal S, Kollmannsberger C, Lee J L, Venugopal B, van den Eertwegh A J M, Negrier S, Gurney H, Albiges L, Berger R, Haanen J B A G, Oyervides Juárez V, Rini B I, Larkin J, Nolè F, Schmidinger M, Atkins M B, Tomita Y, Ellers-Lenz B, Hoffman J, Sandner R, Wang J, di Pietro A, Motzer R J

机构信息

The Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, USA.

Private Medical Institution, Euromedservice, St. Petersburg, Russian Federation.

出版信息

Ann Oncol. 2025 Apr;36(4):387-392. doi: 10.1016/j.annonc.2024.12.008. Epub 2024 Dec 18.

Abstract

BACKGROUND

In the phase III JAVELIN Renal 101 trial (NCT02684006), first-line treatment with avelumab + axitinib resulted in significantly longer progression-free survival (PFS) and a higher objective response rate (ORR) versus sunitinib in patients with advanced renal cell carcinoma (aRCC). We report the final analysis, including the primary analysis of overall survival (OS).

PATIENTS AND METHODS

Patients with untreated aRCC (any prognostic risk score) were enrolled. The primary endpoints were OS and PFS in the programmed death-ligand 1-positive (PD-L1+) population. ORR, duration of response, safety, and patient-reported outcomes (PROs) were also assessed.

RESULTS

The minimum follow-up was 68 months in all patients. The median OS with avelumab + axitinib versus sunitinib, respectively, was 43.2 months [95% confidence interval (CI) 36.5-51.7 months] versus 36.2 months (95% CI 29.8-44.2 months) in the PD-L1+ population [hazard ratio (HR) 0.86 (95% CI 0.701-1.057); P = 0.0755] and 44.8 months (95% CI 39.7-51.1 months) versus 38.9 months (95% CI 31.4-45.2 months) in the overall population [HR 0.88 (95% CI 0.749-1.039); P = 0.0669]. Investigator-assessed PFS remained prolonged with avelumab + axitinib versus sunitinib [5-year event-free rate in the overall population, 12.0% (95% CI 8.9% to 15.6%) versus 4.4% (95% CI 2.5% to 7.3%)]. ORR in the overall population was 59.7% (95% CI 55.0% to 64.3%) with avelumab + axitinib versus 32.0% (95% CI 27.7% to 36.5%) with sunitinib; duration of response was ≥5 years in 16.4% (95% CI 12.0% to 21.4%) versus 9.2% (95% CI 4.6% to 15.7%), respectively. Rates of grade ≥3 treatment-related adverse events were 66.8% versus 61.5%, respectively. PROs were similar between arms.

CONCLUSIONS

JAVELIN Renal 101 provides the longest follow-up to date for immune checkpoint inhibitor + tyrosine kinase inhibitor combination treatment from a phase III trial in aRCC. OS analyses favored avelumab + axitinib versus sunitinib but did not reach statistical significance; subsequent treatment may have impacted results. Avelumab + axitinib provided long-term efficacy benefits versus sunitinib, including prolonged PFS, a nearly doubled ORR, and more durable responses, with a manageable long-term safety profile.

摘要

背景

在III期JAVELIN肾101试验(NCT02684006)中,与舒尼替尼相比,阿维鲁单抗+阿昔替尼一线治疗晚期肾细胞癌(aRCC)患者可显著延长无进展生存期(PFS)并提高客观缓解率(ORR)。我们报告最终分析结果,包括总生存期(OS)的初步分析。

患者与方法

纳入未经治疗的aRCC患者(任何预后风险评分)。主要终点为程序性死亡配体1阳性(PD-L1+)人群的OS和PFS。还评估了ORR、缓解持续时间、安全性和患者报告结局(PRO)。

结果

所有患者的最短随访时间为68个月。在PD-L1+人群中,阿维鲁单抗+阿昔替尼与舒尼替尼相比,中位OS分别为43.2个月[95%置信区间(CI)36.5 - 51.7个月]和36.2个月(95% CI 29.8 - 44.2个月)[风险比(HR)0.86(95% CI 0.701 - 1.057);P = 0.0755];在总体人群中,分别为44.8个月(95% CI 39.7 - 51.1个月)和38.9个月(95% CI 31.4 - 45.2个月)[HR 0.88(95% CI 0.749 - 1.039);P = 0.0669]。研究者评估的PFS方面,阿维鲁单抗+阿昔替尼与舒尼替尼相比仍有延长[总体人群5年无事件发生率,分别为12.0%(95% CI 8.9%至15.6%)和4.4%(95% CI 2.5%至7.3%)]。总体人群中,阿维鲁单抗+阿昔替尼的ORR为59.7%(95% CI 55.0%至64.3%),舒尼替尼为32.0%(95% CI 27.7%至36.5%);缓解持续时间≥5年的比例分别为16.4%(95% CI 12.0%至21.4%)和9.2%(95% CI 4.6%至15.7%)。≥3级治疗相关不良事件发生率分别为66.8%和61.5%。两组的PRO相似。

结论

JAVELIN肾101试验提供了aRCC III期试验中免疫检查点抑制剂+酪氨酸激酶抑制剂联合治疗迄今为止最长的随访数据。OS分析显示阿维鲁单抗+阿昔替尼优于舒尼替尼,但未达到统计学意义;后续治疗可能影响了结果。与舒尼替尼相比,阿维鲁单抗+阿昔替尼具有长期疗效优势,包括延长PFS、ORR几乎翻倍以及更持久的缓解,且长期安全性可控。

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